Preparation and characterization of a self-emulsifying pellet formulation

被引:85
作者
Abdalla, Ahmed [1 ]
Maeder, Karsten [1 ]
机构
[1] Univ Halle Wittenberg, Dept Pharm, Inst Pharmaceut & Biopharmaceut, D-06120 Halle, Germany
关键词
pellets; extrusion/spheronization; self-emulsifying drug delivery systems; poorly water soluble drugs; oral delivery system; ESR;
D O I
10.1016/j.ejpb.2006.11.015
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
The purpose of the current study is to investigate the feasibility of producing solid self-emulsifying pellets using the extrusion/spheronization technique. Pellets were made from a mixture of C18 partial glycerides, Solutol (R) HS15 and microcrystalline cellulose. Pellets with good physical properties (size, shape, friability) and self-emulsifying properties were produced. The pellets were, in contrast to pellets lacking Solutol, able to transfer a lipophilic dye and a spin probe into the aqueous media. The release kinetics and the microenvironment of the pellets during the release process were assessed using electron spin resonance (ESR) spectroscopy. The ESR results showed that the hydrophobic spin probe was localized mainly in the lipid environment all over the release time. Furthermore, the formulation was capable of accelerating the release of the drug diazepam and achieving a diazepam concentration above its saturation solubility. In conclusion, spherical pellets with low friability and self-emulsifying properties can be produced by the standard extrusion/spheronization technique. The pellets are capable of transfering lipophilic compounds into the aqueous phase and have a high potential to increase the bioavailability of lipophilic drugs. (C) 2006 Elsevier B.V. All rights reserved.
引用
收藏
页码:220 / 226
页数:7
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